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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,113
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls
Most common hazardLack of Assurance of Sterility 2,072 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,527 recalls have been announced year to date.
  • Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
  • The highest complete period was Jun 2026 (297).
  • Sep 2026 is incomplete and not included in the figures above.
  • Complete data
  • Incomplete
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 5,021–5,040 of 20,083 recalls

FDA Recall Terminated Historical recordClass I

CVS Health, Magnesium Citrate SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz), Lemon Flavor, 10 FL OZ (296 mL), a) UPC 0 50428 30594 2; b) UPC 0 50428 33517 8; Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895.

by Vi-Jon, LLC

Reason
Microbial contamination of non-sterile products.
Published
September 21, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass I

Banana Boat hair & scalp defense, Clear Sunscreen Spray SPF 30, Avobenzone 2.0%, Homosalate 6.0%, Octocrylene 6.0%, packaged in Net Wt 6 oz. aluminum spray can, Distributed by: Edgewell Personal Care Brands, LLC, Shelton, CT 06484, UPC 0 79656 04041 8

by Edgewell Personal Care Brands, LLC

Reason
Chemical contamination: presence of benzene
Published
September 21, 2022
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

EZ Noble Sushi

Product
California crunch roll (9.6 oz) with expiration 08/12/2022
Reason
Contains undeclared wheat.
Published
September 21, 2022
Distribution
MA and CT

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FDA Recall United States Terminated Historical recordClass I

EZ Noble Sushi

Product
Shrimp tempura & lobster roll (12.8 oz) with expiration 08/1…
Reason
Contains undeclared wheat.
Published
September 21, 2022
Distribution
MA and CT

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FDA Recall United States Terminated Historical recordClass I

EZ Noble Sushi

Product
Pink lady and salmon avocado roll (9 oz) with expiration 08/…
Reason
Contains undeclared egg.
Published
September 21, 2022
Distribution
MA and CT

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FDA Recall United States Terminated Historical recordClass II

EZ Noble Sushi

Product
Philadelphia avocado or cucumber classic roll (8 oz) with ex…
Reason
Contains undeclared milk.
Published
September 21, 2022
Distribution
MA and CT

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FDA Recall United States Terminated Historical recordClass I

EZ Noble Sushi

Product
Spicy shrimp roll (8 oz) with expiration 08/12/2022
Reason
Contains undeclared egg.
Published
September 21, 2022
Distribution
MA and CT

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FDA Recall United States Terminated Historical recordClass I

EZ Noble Sushi

Product
Spicy tuna roll (9.6 oz) with expiration 08/12/2022
Reason
Contains undeclared egg.
Published
September 21, 2022
Distribution
MA and CT

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FDA Recall United States Terminated Historical recordClass I

EZ Noble Sushi

Product
Spicy salmon roll (9.6 oz) with expiration 08/12/2022
Reason
Contains undeclared egg.
Published
September 21, 2022
Distribution
MA and CT

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FDA Recall United States Terminated Historical recordClass I

EZ Noble Sushi

Product
Shrimp Tempura and spice shrimp roll (11.2 oz) with expirati…
Reason
Contains undeclared egg and wheat
Published
September 21, 2022
Distribution
MA and CT

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FDA Recall Terminated Historical recordClass II

Difluprednate Ophthalmic Emulsion, 0.05%, 5 mL bottle, RX only, Manufactured by Cipla Ltd., India, Manufactured for: Cipla USA, Inc., NJ 07059, NDC 69097-341-35.

by CIPLA

Reason
Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Difluprednate Ophthalmic Emulsion, 0.05%, 5 mL bottle, RX only, Manufactured for Exelan Pharmecuticals, Inc., Boca Raton, FL 33432, NDC 76282-708-50.

by CIPLA

Reason
Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Sodium Chloride Ophthalmic Ointment USP, 5%, Sterile, Net Wt 3.5 g (1/8 oz) tube, Mfg by: Akorn, Inc., Lake Forest , IL 600405, NDC 17478-622-35

by Akorn, Inc.

Reason
cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during sterility testing. Scope expanded to include other lots and products which potentially share the same root cause.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Lidocaine Hydrochloride Jelly USP, 2%, Sterile, 30mL tube, Rx only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-711-31

by Akorn, Inc.

Reason
cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during sterility testing. Scope expanded to include other lots and products which potentially share the same root cause.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CORRECTDOSE Children's COUGH & CHEST CONGESTION DM (Guaifenesin 100 mg / Dextromethorphan 5 mg per 5 mL) 2.04FL. OZ (60mL), packaged in 12-5 individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-321-05 UPC 8 60003 67146 7

by Plastikon Healthcare LLC

Reason
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CORRECTDOSE Children's PAIN RELIEF & Fever Reducer, Cherry, (Acetaminophen 160 mg per 5 mL), 2.04 FL.OZ (60mL), packaged in 12-5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-311-05 UPC 8 60003 67145 0

by Plastikon Healthcare LLC

Reason
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CORRECTDOSE Children's ALLERGY RELIEF (Diphenhydramine HCl 12.5 mg per 5 mL), 2.04 FL. OZ (60 mL) packaged in 12- 5mL individual doses, Distributed by Correct Dose Inc, Braintree MA 02184. NDC 62320-302-05 UPC 8 60003 67144 3

by Plastikon Healthcare LLC

Reason
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

GUAIFENESIN AND DEXTROMETHORPHAN 200-20 mg/10 mL, 10 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6980-72

by Plastikon Healthcare LLC

Reason
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Published
September 14, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL, 5 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152. NDC 0904-6844-70

by Plastikon Healthcare LLC

Reason
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Published
September 14, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Diphenhydramine HCl Oral Solution, 25 mg / 10 mL, 10 mL cup, packaged in 10 cups per tray, 10 trays per carton, For Institutional Use Only, Major Pharmaceuticals, 17177 N Laurel Park Dr. Suite 233, Livonia, MI 48152, NDC 0904-6741-72

by Plastikon Healthcare LLC

Reason
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Published
September 14, 2022
Distribution
Nationwide

View recall →

Data last updated:

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.